Search
for
Sort by
Research 811–840 of 1000+
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Distinct transcriptomic landscapes of cutaneous basal cell carcinomas and squamous cell carcinomas
- Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- cDermo-1 misexpression induces dense dermis, feathers, and scales
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Damage of hair follicle stem cells and alteration of keratin expression in external radiation-induced acute alopecia
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Skin transcriptome reveals the intrinsic molecular mechanisms underlying hair follicle cycling in Cashmere goats under natural and shortened photoperiod conditions
- Gene expression profiling analysis reveals fur development in rex rabbits (<i>Oryctolagus cuniculus</i>)
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Genetically modified laboratory mice with sebaceous glands abnormalities
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- The circular RNA circNlgnmediates doxorubicin-inducedcardiac remodeling and fibrosis
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- CircRNA-1926 Promotes the Differentiation of Goat SHF Stem Cells into Hair Follicle Lineage by miR-148a/b-3p/CDK19 Axis
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Transcriptional profiling of putative human epithelial stem cells
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Screening the key genes of hair follicle growth cycle in Inner Mongolian Cashmere goat based on RNA sequencing
- Comprehensive analysis of the expression profiles of mRNA, lncRNA, circRNA, and miRNA in primary hair follicles of coarse sheep fetal skin
- Genome-wide detection and sequence conservation analysis of long non-coding RNA during hair follicle cycle of yak
- Multiomics global landscape of stemness-related gene clusters in adipose-derived mesenchymal stem cells
- Hair follicle stem cell progeny heal blisters while pausing skin development
- Deficiency in Nucleotide Excision Repair Family Gene Activity, Especially ERCC3, Is Associated with Non-Pigmented Hair Fiber Growth
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Identification of functional circRNAs regulating ovarian follicle development in goats